scholarly journals Photocatalytic Degradation of Reactive Yellow in Batch and Continuous Photoreactor Using Titanium Dioxide

2012 ◽  
Vol 4 (3) ◽  
pp. 665-674 ◽  
Author(s):  
M. M. Alam ◽  
M. Z. Bin Mukhlish ◽  
S. Uddin ◽  
S. Das ◽  
K. Ferdous ◽  
...  
Keyword(s):  
Titanium Dioxide ◽  
Layer Thickness ◽  
Catalyst Loading ◽  
Ceramic Plate ◽  
Continuous Mode ◽  
Batch Mode ◽  
Maximum Sorption Capacity ◽  
First Order Kinetics ◽  
Maximum Sorption ◽  
Solution Layer

Titanium dioxide (TiO2) has been used as photo-catalyst for the degradation of reactive yellow (RY) in batch and continuous mode under UV irradiation. Titanium dioxide (TiO2) was immobilized onto the ceramic plate using cement as binder. The effects of various parameters such as initial dye concentration, solution layer thickness, presence of catalyst, residence time, and catalyst loading on degradation have been investigated. The results showed that without catalyst no degradation was achieved. The maximum sorption capacity of TiO2 was found to be 0.01447 kg/kg. The degradation of RY followed pseudo-first order kinetics with rate constant k = 0.001 min-1. A decrease in degradation of RY was observed with an increase in initial concentration and solution layer thickness. A comparison of photocatalytic performance between batch and continuous mode was performed and the batch mode provided better degradation performance. About 60% degradation of dye was achieved at 360 min for 200 ppm RY solution in batch mode.© 2012 JSR Publications. ISSN: 2070-0237 (Print); 2070-0245 (Online). All rights reserved.doi: http://dx.doi.org/10.3329/jsr.v4i3.8654 J. Sci. Res. 4 (3), 665-674 (2012)

Sorption of thallium(I) ions by peat

2013 ◽  
Vol 68 (10) ◽  
pp. 2208-2213 ◽  
Author(s):  
Artis Robalds ◽  
Maris Klavins ◽  
Liga Dreijalte
Keyword(s):  
Sorption Capacity ◽  
Batch Mode ◽  
Maximum Sorption Capacity ◽  
Maximum Sorption ◽  
Pseudo Second Order ◽  
Copper Zinc ◽  
Industrial Use ◽  
Kinetics Of ◽  
Kinetics Of Sorption ◽  
Effective Sorbent

The increasing industrial use of thallium has raised the need for removal of this highly toxic element from wastewater. Thallium is more toxic than cadmium, copper, zinc, lead and mercury and as it is easily accumulated in humans, animals and plants, it poses a threat to both the environment and human health. Peat has been used as an effective, relatively cheap and easily available sorbent to treat waters containing heavy metals. In this study, peat was characterized and used as sorbent for the removal of Tl(I) ions from aqueous solution. The effect of initial Tl(I) concentration, pH, contact time, temperature and ionic strength was studied in batch mode. The maximum sorption capacity of peat reached 24.14 mg/g at 20 °C and initial Tl(I) concentration of 500 mg/L. Sorption capacity was found to be pH dependent and maximum uptake occurred at pH 10. Kinetic data revealed that sorption was relatively rapid – 82.8% of Tl(I) ions were sorbed in the first 10 min. The kinetics of sorption was analyzed using pseudo-first order and pseudo-second order models. Results show that peat can be used as an effective sorbent to remove Tl(I) ions from aqueous solutions.

scholarly journals Magnetized Chitosan Nanocomposite as an Effective Adsorbent for the Removal of Methylene Blue and Malachite Green Dyes

2021 ◽  
Author(s):  
Fouzia Mashkoor ◽  
Abu Nasar
Keyword(s):  
Electron Microscopy ◽  
Methylene Blue ◽  
Malachite Green ◽  
Batch Mode ◽  
X Ray ◽  
Maximum Sorption Capacity ◽  
Transmission Electron ◽  
Maximum Sorption ◽  
Equilibrium Data ◽  
Adsorption Equilibrium Data

Abstract Herein, a magnetically separable Fe3O4 decorated chitosan was facilely synthesized, systematically characterized, and subsequently employed as a versatile adsorbing material for the adsorption of malachite green and methylene blue dyes. The prepared adsorbent was characteristically examined through Fourier transform infra-red microscopy, scanning electron microscopy with energy-dispersive X-ray analysis, transmission electron microscopy X-ray diffraction, Brunauere-Emmette-Teller surface area analysis, thermogravimetric analysis, and vibrating-sample magnetometry techniques. The performance of adsorbent was studied in batch mode and the the time-dependent experimental data were analyzed with different kinetic models, and pseudo-IInd-order was provided the best fit for the adsorption of both the dyes with a high value of the regression coefficient. The adsorption equilibrium data of both the dyes was best explained by Langmuir isotherm, and the maximum sorption capacity of MG and MB was found to be 55.86 and 76.34 mg g-1, respectively. Thermodynamic analysis declared that the adsorption of MG and MB onto the MChi was endothermic and spontaneous in nature. Moreover, the adsorbent presented good reusability up to three successive ad-/de-sorption cycles, indicating that MChi is a promising applicant for the treatment of dye-containing wastewater.

Removal of nickel(II) from aqueous solution by Vigna unguiculata (cowpea) pods biomass

2016 ◽  
Vol 73 (10) ◽  
pp. 2301-2310 ◽  
Author(s):  
Upenyu Guyo ◽  
Kudakwashe Sibanda ◽  
Edith Sebata ◽  
Fidelis Chigondo ◽  
Mambo Moyo
Keyword(s):  
Aqueous Solution ◽  
Correlation Coefficient ◽  
Vigna Unguiculata ◽  
Order Model ◽  
Batch Mode ◽  
Maximum Sorption Capacity ◽  
Biosorption Process ◽  
Chi Squared ◽  
Maximum Sorption ◽  
Pseudo Second Order

The potential to remove nickel(II) ions from aqueous solution using a biosorbent prepared from Vigna unguiculata pods (VUPs) was investigated in batch experiments. The batch mode experiments were conducted utilising the independent variables of pH (2 to 8), contact time (5 to 120 min), dosage concentration (0.2 to 1.6 g), nickel(II) concentrations (10 to 80 mg L−1) and temperature (20 to 50°C). The biosorption data fitted best to the Freundlich biosorption model with a correlation coefficient (R2) of 0.993 and lowest chi-squared value of 31.89. The maximum sorption capacity of the VUP for nickel(II) was 27.70 mg g−1. Kinetics studies revealed that the biosorption process followed the pseudo-second-order model as it had the lowest sum of square error value (0.808) and correlation coefficient close to unity (R2 = 0.998). The calculated thermodynamic parameters showed that the biosorption process was feasible, spontaneous and endothermic. Consequently, the study demonstrated that VUP biomass could be used as a biosorbent for the removal of nickel(II) from aqueous solution.

Природные материалы для сорбционной очистки хром- и кадмийсодержащих инфильтратов полигонов ТБО

2019 ◽  
pp. 13-19
Author(s):  
A. Safonov ◽  
N. Andriushchenko ◽  
N. Popova ◽  
K. Boldyrev
Keyword(s):  
Sorption Capacity ◽  
Electron Acceptors ◽  
Bacterial Cells ◽  
Maximum Sorption Capacity ◽  
Sorption Material ◽  
Maximum Sorption ◽  
Properties Of Materials ◽  
Solid Waste Landfills ◽  
Sorption Characteristics

Проведен анализ сорбционных характеристик природных материалов (вермикулит, керамзит, перлит, цеолит Трейд ) при очистке кадмий- и хромсодержащих сточных вод с высокой нагрузкой по ХПК. Установлено, что цеолит обладает максимальными сорбционными характеристиками для Cd и Cr и наименьшим биологическим обрастанием. При использовании вермикулита и керамзита или смесей на их основе можно ожидать увеличения сорбционной емкости для Cd и Сr при микробном обрастании, неизбежно происходящем в условиях контакта с водами, загрязненными органическими соединениями и биогенами. При этом биообрастание может повысить иммобилизационную способность материалов для редоксзависимых металлов за счет ферментативных ресурсов бактериальных клеток, использующих их в качестве акцепторов электронов. Эффект микробного обрастания разнонаправленно изменял параметры материалов: для Cr в большинстве случаев уменьшение и для Cd значительное увеличение. При этом дополнительным эффектом иммобилизации Cr является его биологическое восстановление биопленками. Варьируя состав сорбционного материала, можно подбирать смеси, оптимально подходящие для очистки вод инфильтратов с полигонов твердых бытовых отходов с высокой нагрузкой по ХПК и биогенным элементам как при использовании in situ, так и в системах на поверхности.The analysis of the sorption characteristics of natural materials (vermiculite, expanded clay, perlite, Trade zeolite) during the purification of cadmium and chromium-containing leachate with a high COD load was carried out. It was determined that zeolite had the maximum sorption capacity for Cd and Cr and the lowest biological fouling. When using vermiculite and expanded clay or mixtures on their basis, one can expect an increase in the sorption capacity for Cd and Cr during microbial fouling that inevitably occurs during contacting with water polluted with organic compounds and nutrients. In this case biofouling can increase the immobilization properties of materials for redox-dependent metals due to the enzymatic resources of bacterial cells that use them as electron acceptors. The effect of microbial fouling changed the parameters of materials in different directions: for Cr, in most cases, downward, and for Cd, significantly upward. Moreover, chromium biological recovery by biofilms is an additional effect of immobilization. Varying the composition of the sorption material provides for selecting mixtures that are optimally suitable for the purification of leachates from solid waste landfills with high COD and nutrients load, both when used in situ and in surface systems.

Growth Characteristics of Activated Sludges Acclimated to para-Nitrophenol in Batch and Continuous Modes

1994 ◽  
Vol 29 (7) ◽  
pp. 327-333
Author(s):  
Y. Matsui ◽  
F. Yamaguchi ◽  
Y. Suwa ◽  
Y. Urushigawa
Keyword(s):  
Growth Characteristics ◽  
The Other ◽  
Operational Mode ◽  
Continuous Mode ◽  
Relative Resistance ◽  
Batch Mode ◽  
The Given ◽  
Operational Modes ◽  
Very High ◽  
Sensitive Group

Activated sludges were acclimated to p-nitrophenol (PNP) in two operational modes, a batch and a continuous. The operational mode of the PNP acclimation of activated sludges strongly affected the physiological characteristics of predominant microorganisms responsible for PNP degradation. Predominant PNP degraders in the sludge in batch mode (Sludge B) had lower PNP affinity and were relatively insensitive to PNP concentration. Those of the sludge in continuous mode (Sludge C), on the other hand, had very high PNP affinity and were sensitive to PNP. MPN enumeration of PNP degraders in sludge B and C using media with different PNP concentrations (0.05, 0.2,0.5 and 2.0 mM) supported the above results. Medium with 0.2 mM of PNP did not recover PNP degraders in sludge C well, while it recovered PNP degraders in sludge B as well as the medium with 0.05 mM did. When switching from one operational mode to the other, the predominant population in sludge B shifted to the sensitive group, but that of sludge C did not shift at the given loading of PNP, showing relative resistance to inhibitive concentration.

scholarly journals Phosphate Removal Using Polyethylenimine Functionalized Silica-Based Materials

2021 ◽  
Vol 13 (3) ◽  
pp. 1502
Author(s):  
Maria Xanthopoulou ◽  
Dimitrios Giliopoulos ◽  
Nikolaos Tzollas ◽  
Konstantinos S. Triantafyllidis ◽  
Margaritis Kostoglou ◽  
...  
Keyword(s):  
Sorption Capacity ◽  
Removal Rate ◽  
Phosphate Concentration ◽  
Phosphate Removal ◽  
Equilibrium Studies ◽  
Maximum Sorption Capacity ◽  
Algae Blooms ◽  
Maximum Sorption ◽  
Phosphate Anions ◽  
Adsorbent Dose

In water and wastewater, phosphate anions are considered critical contaminants because they cause algae blooms and eutrophication. The present work aims at studying the removal of phosphate anions from aqueous solutions using silica particles functionalized with polyethylenimine. The parameters affecting the adsorption process such as pH, initial concentration, adsorbent dose, and the presence of competitive anions, such as carbonate, nitrate, sulfate and chromate ions, were studied. Equilibrium studies were carried out to determine their sorption capacity and the rate of phosphate ions uptake. The adsorption isotherm data fitted well with the Langmuir and Sips model. The maximum sorption capacity was 41.1 mg/g at pH 5, which decreased slightly at pH 7. The efficiency of phosphate removal adsorption increased at lower pH values and by increasing the adsorbent dose. The maximum phosphate removal was 80% for pH 5 and decreased to 75% for pH 6, to 73% for pH 7 and to 70% for pH 8, for initial phosphate concentration at about 1 mg/L and for a dose of adsorbent 100 mg/L. The removal rate was increased with the increase of the adsorbent dose. For example, for initial phosphate concentration of 4 mg/L the removal rate increased from 40% to 80% by increasing the dose from 0.1 to 2.0 g/L at pH 7. The competitive anions adversely affected phosphate removal. Though they were also found to be removed to a certain extent. Their co-removal provided an adsorbent which might be very useful for treating waters with low-level multiple contaminant occurrence in natural or engineered aquatic systems.

scholarly journals Modified Exfoliated Carbon Nanoplatelets as Sorbents for Ammonium from Natural Mineral Waters

Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3541
Author(s):  
Ion Ion ◽  
Daniela Bogdan ◽  
Monica Maria Mincu ◽  
Alina Catrinel Ion
Keyword(s):  
Natural Waters ◽  
Mineral Waters ◽  
Aqueous Samples ◽  
Sorption Mechanism ◽  
Characteristic Parameters ◽  
Sorption Characteristic ◽  
Natural Mineral ◽  
Maximum Sorption Capacity ◽  
Ammonium Removal ◽  
Maximum Sorption

In this manuscript an improved sorbent based on modified exfoliated carbon nanoplatelets, applied in the removal of ammonium from aqueous samples, is presented. This sorbent showed better efficiency in comparison with the previous one obtained in our group for ammonium removal, the values of the maximum sorption capacity being improved from 10 to 12.04 mg/g. In terms of kinetics and sorption characteristic parameters, their values were also improved. Based on these results, a sorption mechanism was proposed, taking into account ion-exchange and chemisorption processes at the surface of the oxidized exfoliated carbon nanoplatelets. Future applications for simultaneous removal of other positive charged contaminants from natural waters might be possible.

scholarly journals Batch and Semi-Continuous Anaerobic Digestion of Industrial Solid Citrus Waste for the Production of Bioenergy

Processes ◽  
2021 ◽  
Vol 9 (4) ◽  
pp. 648
Author(s):  
Erik Samuel Rosas-Mendoza ◽  
Andrea Alvarado-Vallejo ◽  
Norma Alejandra Vallejo-Cantú ◽  
Raúl Snell-Castro ◽  
Sergio Martínez-Hernández ◽  
...  
Keyword(s):  
Anaerobic Digestion ◽  
Oxygen Demand ◽  
Continuous Mode ◽  
Citrus Industry ◽  
Batch Mode ◽  
Volatile Solids ◽  
Working Volume ◽  
Plant Level ◽  
Citrus Waste ◽  
Mesophilic Conditions

The aim of this paper is to describe a study of the anaerobic digestion of industrial citrus solid waste (ISCW) in both batch and semi-continuous modes for the production of bioenergy without the elimination of D-limonene. The study was conducted at the pilot plant level in an anaerobic reactor with a working volume of 220 L under mesophilic conditions of 35 ± 2 °C. Cattle manure (CM) was used as the inoculum. Three batches were studied. The first batch had a CM/ISCW ratio of 90/10, and Batches 2 and 3 had CM/ISCW ratios of 80/20 and 70/30, respectively. In the semi-continuous mode an OLR of approximately 8 g total chemical oxygen demand (COD)/Ld (4.43 gVS/Ld) was used. The results showed that 49%, 44%, and 60% of volatile solids were removed in the batch mode, and 35% was removed in the semi-continuous mode. In the batch mode, 0.322, 0.382, and 0.316 LCH4 were obtained at STP/gVSremoved. A total of 24.4 L/d (34% methane) was measured in the semi-continuous mode. Bioenergy potentials of 3.97, 5.66, and 8.79 kWh were obtained for the respective batches, and 0.09 kWh was calculated in the semi-continuous mode. The citrus industry could produce 37 GWh per season. A ton of processed oranges has a bioenergy potential of 162 kWh, which is equivalent to 49 kWh of available electricity ($3.90).

Sorption Profile of Hg(II) onto Mixed Phase of Copper Sulphide and Copper Sulphate

2011 ◽  
Vol 356-360 ◽  
pp. 537-546
Author(s):  
Yow Loo Au Yoong ◽  
Pei Lay Yap ◽  
Muralithran G. Kutty ◽  
Olaf Timpe ◽  
Malte Behrens ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Copper Sulphate ◽  
Surface Complexation ◽  
Mixed Phase ◽  
Copper Sulphide ◽  
Reaction Parameters ◽  
Sorption Behaviour ◽  
Maximum Sorption Capacity ◽  
Maximum Sorption ◽  
Equilibrium Data

The use of surface oxidized covellite (CuS), namely mixed phase copper sulphide (CuS and CuSO4) was studied for the removal of mercury from aqueous solution under the effect of various reaction parameters (pH, time, Hg(II) concentration). From batch sorption studies, the equilibrium data revealed that the sorption behaviour of Hg(II) onto mixed phase copper sulphide follows well with Langmuir isotherm and the maximum sorption capacity (Qmax) determined ≈ 400mg Hg(II) /g of sorbent. Meanwhile, all the unreacted and reacted mixed phase copper sulphides were also characterized by Powder XRD, SEM and XPS techniques. The results indicated that the sorption of Hg(II) onto mixed phase copper sulphide occurs initially through the dissolution of surface oxidized CuSO4layer. After that, the surface complexation product formed and sorbed onto the surface of CuS. These outcomes suggest the potential ability of CuS in removing Hg(II) even if the CuS layer is being surrounded by oxidized layer of CuSO4.

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